JP2008533176A - ケラチン繊維のための還元着色系 - Google Patents
ケラチン繊維のための還元着色系 Download PDFInfo
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- JP2008533176A JP2008533176A JP2008502156A JP2008502156A JP2008533176A JP 2008533176 A JP2008533176 A JP 2008533176A JP 2008502156 A JP2008502156 A JP 2008502156A JP 2008502156 A JP2008502156 A JP 2008502156A JP 2008533176 A JP2008533176 A JP 2008533176A
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- Prior art keywords
- group
- amino
- substituted
- carbaldehyde
- hydroxy
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- 239000000835 fiber Substances 0.000 title claims abstract description 13
- 102000011782 Keratins Human genes 0.000 title claims abstract description 11
- 108010076876 Keratins Proteins 0.000 title claims abstract description 11
- 238000004040 coloring Methods 0.000 title claims description 8
- -1 cationic oxime ester Chemical class 0.000 claims abstract description 62
- 210000004209 hair Anatomy 0.000 claims abstract description 25
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims abstract description 22
- 150000001728 carbonyl compounds Chemical class 0.000 claims abstract description 16
- 239000000118 hair dye Substances 0.000 claims abstract description 10
- 235000010323 ascorbic acid Nutrition 0.000 claims abstract description 9
- 239000011668 ascorbic acid Substances 0.000 claims abstract description 9
- 229960005070 ascorbic acid Drugs 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims abstract description 9
- 238000004043 dyeing Methods 0.000 claims abstract description 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 33
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 27
- 239000003086 colorant Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 22
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 13
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 11
- 125000003277 amino group Chemical group 0.000 claims description 10
- 125000002091 cationic group Chemical group 0.000 claims description 9
- 229920006395 saturated elastomer Polymers 0.000 claims description 9
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 125000000623 heterocyclic group Chemical group 0.000 claims description 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 7
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- 239000000982 direct dye Substances 0.000 claims description 5
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims description 5
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 4
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 claims description 4
- 125000005001 aminoaryl group Chemical group 0.000 claims description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 4
- 125000005392 carboxamide group Chemical group NC(=O)* 0.000 claims description 4
- 125000005518 carboxamido group Chemical group 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 230000003750 conditioning effect Effects 0.000 claims description 4
- 239000002537 cosmetic Substances 0.000 claims description 4
- 239000000975 dye Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 229920005615 natural polymer Polymers 0.000 claims description 4
- RMVRSNDYEFQCLF-UHFFFAOYSA-N phenyl mercaptan Natural products SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 claims description 4
- 229920000642 polymer Polymers 0.000 claims description 4
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 4
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 4
- RADKZDMFGJYCBB-UHFFFAOYSA-N Pyridoxal Chemical compound CC1=NC=C(CO)C(C=O)=C1O RADKZDMFGJYCBB-UHFFFAOYSA-N 0.000 claims description 3
- XKSWHQSEMXBLNM-UHFFFAOYSA-M [(1,3-dioxoinden-2-ylidene)amino] 2-[4-(dimethylamino)pyridin-1-ium-1-yl]acetate;bromide Chemical compound [Br-].C1=CC(N(C)C)=CC=[N+]1CC(=O)ON=C1C(=O)C2=CC=CC=C2C1=O XKSWHQSEMXBLNM-UHFFFAOYSA-M 0.000 claims description 3
- 239000002453 shampoo Substances 0.000 claims description 3
- 229920001059 synthetic polymer Polymers 0.000 claims description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 3
- KAESVJOAVNADME-UHFFFAOYSA-N 1H-pyrrole Natural products C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 2
- TYLGFSQJWWRSKH-UHFFFAOYSA-N 3-methyl-1-pyridin-2-yl-5-pyrrol-1-ylpyrazole-4-carbaldehyde Chemical compound O=CC=1C(C)=NN(C=2N=CC=CC=2)C=1N1C=CC=C1 TYLGFSQJWWRSKH-UHFFFAOYSA-N 0.000 claims description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Natural products C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 2
- NCYCYZXNIZJOKI-OVSJKPMPSA-N Retinaldehyde Chemical compound O=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-OVSJKPMPSA-N 0.000 claims description 2
- YIJLYHNWJWQIMB-UHFFFAOYSA-M [(1,3-dioxoinden-2-ylidene)amino] 2-(3-methylimidazol-3-ium-1-yl)acetate;bromide Chemical compound [Br-].C1=[N+](C)C=CN1CC(=O)ON=C1C(=O)C2=CC=CC=C2C1=O YIJLYHNWJWQIMB-UHFFFAOYSA-M 0.000 claims description 2
- BDFBTMCXTCPNGU-UHFFFAOYSA-M [(4,5,6,7-tetrachloro-1,3-dioxoinden-2-ylidene)amino] 2-[4-(dimethylamino)pyridin-1-ium-1-yl]acetate;bromide Chemical compound [Br-].C1=CC(N(C)C)=CC=[N+]1CC(=O)ON=C1C(=O)C2=C(Cl)C(Cl)=C(Cl)C(Cl)=C2C1=O BDFBTMCXTCPNGU-UHFFFAOYSA-M 0.000 claims description 2
- VUIGUBLHAXSCOE-GOSREXKOSA-M [(e)-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)amino] 2-[4-(dimethylamino)pyridin-1-ium-1-yl]acetate;bromide Chemical compound [Br-].C1=CC(N(C)C)=CC=[N+]1CC(=O)O\N=C/1C(=O)N(C=2C=CC=CC=2)N=C\1C VUIGUBLHAXSCOE-GOSREXKOSA-M 0.000 claims description 2
- QGBZBIRPUSIPTI-ZUQRMPMESA-M [(e)-(4-nitro-1,3-dioxoinden-2-ylidene)amino] 2-(3-methylimidazol-3-ium-1-yl)acetate;bromide Chemical compound [Br-].C1=[N+](C)C=CN1CC(=O)O\N=C/1C(=O)C2=C([N+]([O-])=O)C=CC=C2C\1=O QGBZBIRPUSIPTI-ZUQRMPMESA-M 0.000 claims description 2
- RHXZSTFDEUOUJF-PXMDEAMVSA-M [(e)-(4-nitro-1,3-dioxoinden-2-ylidene)amino] 2-[4-(dimethylamino)pyridin-1-ium-1-yl]acetate;bromide Chemical compound [Br-].C1=CC(N(C)C)=CC=[N+]1CC(=O)O\N=C/1C(=O)C2=C([N+]([O-])=O)C=CC=C2C\1=O RHXZSTFDEUOUJF-PXMDEAMVSA-M 0.000 claims description 2
- LFGSBMHKOYOGSI-SJEOTZHBSA-M [(e)-(5-methoxy-1,3-dioxoinden-2-ylidene)amino] 2-[4-(dimethylamino)pyridin-1-ium-1-yl]acetate;bromide Chemical compound [Br-].C=1C(OC)=CC=C(C2=O)C=1C(=O)\C2=N\OC(=O)C[N+]1=CC=C(N(C)C)C=C1 LFGSBMHKOYOGSI-SJEOTZHBSA-M 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 239000001000 anthraquinone dye Substances 0.000 claims description 2
- 150000005840 aryl radicals Chemical class 0.000 claims description 2
- 239000000987 azo dye Substances 0.000 claims description 2
- 239000000981 basic dye Substances 0.000 claims description 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N benzopyrrole Natural products C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 claims description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 2
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 claims description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 2
- 150000002500 ions Chemical class 0.000 claims description 2
- 239000001005 nitro dye Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000005496 phosphonium group Chemical group 0.000 claims description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N protonated dimethyl amine Natural products CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 2
- 150000003254 radicals Chemical class 0.000 claims description 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 2
- 125000004962 sulfoxyl group Chemical group 0.000 claims description 2
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 claims description 2
- NCYCYZXNIZJOKI-UHFFFAOYSA-N vitamin A aldehyde Natural products O=CC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C NCYCYZXNIZJOKI-UHFFFAOYSA-N 0.000 claims description 2
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims 4
- BTQAJGSMXCDDAJ-UHFFFAOYSA-N 2,4,6-trihydroxybenzaldehyde Chemical compound OC1=CC(O)=C(C=O)C(O)=C1 BTQAJGSMXCDDAJ-UHFFFAOYSA-N 0.000 claims 2
- IUNJCFABHJZSKB-UHFFFAOYSA-N 2,4-dihydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C(O)=C1 IUNJCFABHJZSKB-UHFFFAOYSA-N 0.000 claims 2
- RGHHSNMVTDWUBI-UHFFFAOYSA-N 4-hydroxybenzaldehyde Chemical compound OC1=CC=C(C=O)C=C1 RGHHSNMVTDWUBI-UHFFFAOYSA-N 0.000 claims 2
- OLNJUISKUQQNIM-UHFFFAOYSA-N indole-3-carbaldehyde Chemical compound C1=CC=C2C(C=O)=CNC2=C1 OLNJUISKUQQNIM-UHFFFAOYSA-N 0.000 claims 2
- JVTZFYYHCGSXJV-UHFFFAOYSA-N isovanillin Chemical compound COC1=CC=C(C=O)C=C1O JVTZFYYHCGSXJV-UHFFFAOYSA-N 0.000 claims 2
- ZRSNZINYAWTAHE-UHFFFAOYSA-N p-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C=C1 ZRSNZINYAWTAHE-UHFFFAOYSA-N 0.000 claims 2
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims 2
- WJUFSDZVCOTFON-UHFFFAOYSA-N veratraldehyde Chemical compound COC1=CC=C(C=O)C=C1OC WJUFSDZVCOTFON-UHFFFAOYSA-N 0.000 claims 2
- UWTZBVTWSKWXMN-VDESZNBCSA-N (2e,4e)-5-phenylpenta-2,4-dienal Chemical compound O=C\C=C\C=C\C1=CC=CC=C1 UWTZBVTWSKWXMN-VDESZNBCSA-N 0.000 claims 1
- ALGQVMMYDWQDEC-OWOJBTEDSA-N (e)-3-(4-nitrophenyl)prop-2-enal Chemical compound [O-][N+](=O)C1=CC=C(\C=C\C=O)C=C1 ALGQVMMYDWQDEC-OWOJBTEDSA-N 0.000 claims 1
- KXYBYRKRRGSZCX-UHFFFAOYSA-N 1-methylindole-3-carbaldehyde Chemical compound C1=CC=C2N(C)C=C(C=O)C2=C1 KXYBYRKRRGSZCX-UHFFFAOYSA-N 0.000 claims 1
- SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 claims 1
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims 1
- IXWOUPGDGMCKGT-UHFFFAOYSA-N 2,3-dihydroxybenzaldehyde Chemical group OC1=CC=CC(C=O)=C1O IXWOUPGDGMCKGT-UHFFFAOYSA-N 0.000 claims 1
- AFUKNJHPZAVHGQ-UHFFFAOYSA-N 2,5-dimethoxy-Benzaldehyde Chemical compound COC1=CC=C(OC)C(C=O)=C1 AFUKNJHPZAVHGQ-UHFFFAOYSA-N 0.000 claims 1
- MXZAONCKLBCRQJ-UHFFFAOYSA-N 3-methyl-1-phenyl-5-pyrrolidin-1-ylpyrazole-4-carbaldehyde Chemical compound O=CC=1C(C)=NN(C=2C=CC=CC=2)C=1N1CCCC1 MXZAONCKLBCRQJ-UHFFFAOYSA-N 0.000 claims 1
- HGWZWKWGSIPYDJ-UHFFFAOYSA-N 3-methyl-5-morpholin-4-yl-1-phenylpyrazole-4-carbaldehyde Chemical compound O=CC=1C(C)=NN(C=2C=CC=CC=2)C=1N1CCOCC1 HGWZWKWGSIPYDJ-UHFFFAOYSA-N 0.000 claims 1
- MRLGCTNJRREZHZ-UHFFFAOYSA-N 3-phenoxybenzaldehyde Chemical compound O=CC1=CC=CC(OC=2C=CC=CC=2)=C1 MRLGCTNJRREZHZ-UHFFFAOYSA-N 0.000 claims 1
- BGNGWHSBYQYVRX-UHFFFAOYSA-N 4-(dimethylamino)benzaldehyde Chemical compound CN(C)C1=CC=C(C=O)C=C1 BGNGWHSBYQYVRX-UHFFFAOYSA-N 0.000 claims 1
- RUKJCCIJLIMGEP-ONEGZZNKSA-N 4-dimethylaminocinnamaldehyde Chemical compound CN(C)C1=CC=C(\C=C\C=O)C=C1 RUKJCCIJLIMGEP-ONEGZZNKSA-N 0.000 claims 1
- MVXMNHYVCLMLDD-UHFFFAOYSA-N 4-methoxynaphthalene-1-carbaldehyde Chemical compound C1=CC=C2C(OC)=CC=C(C=O)C2=C1 MVXMNHYVCLMLDD-UHFFFAOYSA-N 0.000 claims 1
- OHMZZAKYOVIFRR-UHFFFAOYSA-N CN(C)c1ccc2C(=O)C(C=O)=C(O)c2c1 Chemical compound CN(C)c1ccc2C(=O)C(C=O)=C(O)c2c1 OHMZZAKYOVIFRR-UHFFFAOYSA-N 0.000 claims 1
- WOPXNXWHIWVGBT-UHFFFAOYSA-N CN1C2C(C(=O)C(C=O)=C2O)c2ccccc12 Chemical compound CN1C2C(C(=O)C(C=O)=C2O)c2ccccc12 WOPXNXWHIWVGBT-UHFFFAOYSA-N 0.000 claims 1
- JGSCUSOWQROCNZ-UHFFFAOYSA-N COc1ccc2C(=O)C(C=O)=C(O)c2c1 Chemical compound COc1ccc2C(=O)C(C=O)=C(O)c2c1 JGSCUSOWQROCNZ-UHFFFAOYSA-N 0.000 claims 1
- KXOYMJARPNPSOJ-UHFFFAOYSA-N COc1ccc2C(=O)C(C=O)=C(O)c2c1OC Chemical compound COc1ccc2C(=O)C(C=O)=C(O)c2c1OC KXOYMJARPNPSOJ-UHFFFAOYSA-N 0.000 claims 1
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims 1
- ODHDUXDTAIMYIE-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2c1ccc1ccccc21 Chemical compound OC1=C(C=O)C(=O)c2c1ccc1ccccc21 ODHDUXDTAIMYIE-UHFFFAOYSA-N 0.000 claims 1
- RBFXCZZVESPPNZ-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2ccc(cc12)[N+]([O-])=O Chemical compound OC1=C(C=O)C(=O)c2ccc(cc12)[N+]([O-])=O RBFXCZZVESPPNZ-UHFFFAOYSA-N 0.000 claims 1
- KBUHNYOCMHFAQD-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2ccccc12 Chemical compound OC1=C(C=O)C(=O)c2ccccc12 KBUHNYOCMHFAQD-UHFFFAOYSA-N 0.000 claims 1
- YFYIBVKRLZLINT-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2cccnc12 Chemical compound OC1=C(C=O)C(=O)c2cccnc12 YFYIBVKRLZLINT-UHFFFAOYSA-N 0.000 claims 1
- ZWHWXQDLXNBOAE-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2ccncc12 Chemical compound OC1=C(C=O)C(=O)c2ccncc12 ZWHWXQDLXNBOAE-UHFFFAOYSA-N 0.000 claims 1
- RRDVOOFJEIQSBW-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2nc3ccccc3nc12 Chemical compound OC1=C(C=O)C(=O)c2nc3ccccc3nc12 RRDVOOFJEIQSBW-UHFFFAOYSA-N 0.000 claims 1
- WSZNBAYOTNFPIH-UHFFFAOYSA-N OC1=C(C=O)C(=O)c2sccc12 Chemical compound OC1=C(C=O)C(=O)c2sccc12 WSZNBAYOTNFPIH-UHFFFAOYSA-N 0.000 claims 1
- KFUJUTFTRXYQMG-UHFFFAOYSA-N bis[4-(dimethylamino)phenyl]methanethione Chemical compound C1=CC(N(C)C)=CC=C1C(=S)C1=CC=C(N(C)C)C=C1 KFUJUTFTRXYQMG-UHFFFAOYSA-N 0.000 claims 1
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- JZMJDSHXVKJFKW-UHFFFAOYSA-N methyl sulfate Chemical compound COS(O)(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-N 0.000 claims 1
- KUCOHFSKRZZVRO-UHFFFAOYSA-N terephthalaldehyde Chemical compound O=CC1=CC=C(C=O)C=C1 KUCOHFSKRZZVRO-UHFFFAOYSA-N 0.000 claims 1
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- 239000000126 substance Substances 0.000 description 7
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- RFQSMLBZXQOMKK-UHFFFAOYSA-N [3-[(4,8-diamino-6-bromo-1,5-dioxonaphthalen-2-yl)amino]phenyl]-trimethylazanium;chloride Chemical compound [Cl-].C[N+](C)(C)C1=CC=CC(NC=2C(C3=C(N)C=C(Br)C(=O)C3=C(N)C=2)=O)=C1 RFQSMLBZXQOMKK-UHFFFAOYSA-N 0.000 description 3
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- MLVYOYVMOZFHIU-UHFFFAOYSA-M sodium;4-[(4-anilinophenyl)diazenyl]benzenesulfonate Chemical compound [Na+].C1=CC(S(=O)(=O)[O-])=CC=C1N=NC(C=C1)=CC=C1NC1=CC=CC=C1 MLVYOYVMOZFHIU-UHFFFAOYSA-M 0.000 description 1
- STZCRXQWRGQSJD-UHFFFAOYSA-N sodium;4-[[4-(dimethylamino)phenyl]diazenyl]benzenesulfonic acid Chemical compound [Na+].C1=CC(N(C)C)=CC=C1N=NC1=CC=C(S(O)(=O)=O)C=C1 STZCRXQWRGQSJD-UHFFFAOYSA-N 0.000 description 1
- MZSDGDXXBZSFTG-UHFFFAOYSA-M sodium;benzenesulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC=CC=C1 MZSDGDXXBZSFTG-UHFFFAOYSA-M 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical group CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- RXJKFRMDXUJTEX-UHFFFAOYSA-N triethylphosphine Chemical group CCP(CC)CC RXJKFRMDXUJTEX-UHFFFAOYSA-N 0.000 description 1
- YWWDBCBWQNCYNR-UHFFFAOYSA-N trimethylphosphine Chemical group CP(C)C YWWDBCBWQNCYNR-UHFFFAOYSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 235000019155 vitamin A Nutrition 0.000 description 1
- 239000011719 vitamin A Substances 0.000 description 1
- 229940045997 vitamin a Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
- Chemical Or Physical Treatment Of Fibers (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05007230A EP1707188B1 (de) | 2005-04-02 | 2005-04-02 | System zum reduktiven Färben von Keratinfasern |
| PCT/US2006/010283 WO2006107594A1 (en) | 2005-04-02 | 2006-03-21 | Reductive colouring system for keratin fibres |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2008533176A true JP2008533176A (ja) | 2008-08-21 |
Family
ID=35044636
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008502156A Pending JP2008533176A (ja) | 2005-04-02 | 2006-03-21 | ケラチン繊維のための還元着色系 |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20060242772A1 (de) |
| EP (1) | EP1707188B1 (de) |
| JP (1) | JP2008533176A (de) |
| CN (1) | CN101151014A (de) |
| AT (1) | ATE368446T1 (de) |
| AU (1) | AU2006232897A1 (de) |
| BR (1) | BRPI0609557A2 (de) |
| CA (1) | CA2601084A1 (de) |
| DE (1) | DE602005001848T2 (de) |
| ES (1) | ES2290806T3 (de) |
| WO (1) | WO2006107594A1 (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2954159B1 (fr) * | 2009-12-22 | 2012-02-10 | Oreal | Agent de coloration et/ou de decoloration des fibres keratiniques comprenant une composition comprenant un agent alcalinisant et une composition anhydre comprenant un oxydant, l'une ou l'autre des compositions pouvant contenir un corps gras |
Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02104778A (ja) * | 1988-09-12 | 1990-04-17 | Bristol Myers Squibb Co | 新規な染色用組成物と染色法 |
| JPH04338321A (ja) * | 1991-02-01 | 1992-11-25 | L'oreal Sa | ケラチン繊維用染色剤 |
| JPH04360818A (ja) * | 1991-03-05 | 1992-12-14 | L'oreal Sa | ケラチン繊維の染色方法および染色剤 |
| JPH04368318A (ja) * | 1991-03-05 | 1992-12-21 | L'oreal Sa | ケラチン繊維の染色方法および染色剤 |
| JPH0597778A (ja) * | 1991-10-03 | 1993-04-20 | Kawasaki Steel Corp | ２−アミノインダンおよびその塩類の製造方法 |
| JPH07508035A (ja) * | 1992-05-20 | 1995-09-07 | メルク エンド カンパニー インコーポレーテッド | ４−アザステロイド５α−レダクターゼ阻害剤 |
| JPH08509479A (ja) * | 1993-04-30 | 1996-10-08 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン | ケラチン含有繊維を染色するためのイサチン誘導体 |
| JPH09510226A (ja) * | 1994-03-17 | 1997-10-14 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのイサチン誘導体 |
| JP2001519369A (ja) * | 1997-10-14 | 2001-10-23 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのインダノン化合物の使用 |
| JP2003128635A (ja) * | 2001-10-16 | 2003-05-08 | Koei Chem Co Ltd | 不飽和アミン類の製造方法 |
| JP2003518481A (ja) * | 1999-12-24 | 2003-06-10 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのメチルキノリニウム化合物の使用 |
| JP2003532743A (ja) * | 2000-05-10 | 2003-11-05 | ウエラ アクチェンゲゼルシャフト | 繊維を染色する薬剤及び繊維を一時的に染色するための方法 |
| JP2005523914A (ja) * | 2002-04-26 | 2005-08-11 | ウエラ アクチェンゲゼルシャフト | ケラチン繊維の酸化染色剤 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL284202A (de) * | 1961-10-26 | 1900-01-01 | ||
| DE19717280A1 (de) * | 1997-04-24 | 1998-10-29 | Henkel Kgaa | Verwendung von heterocyclischen Carbonylverbindungen zum Färben von keratinhaltigen Fasern |
| ES2214055T3 (es) * | 1998-12-07 | 2004-09-01 | Wella Aktiengesellschaft | Producto para el teñido de fibras. |
| WO2001013882A1 (en) * | 1999-08-24 | 2001-03-01 | The Procter & Gamble Company | Methods of lightening keratinous tissue by topical application of oxime compound containing compositions |
| DE10241076A1 (de) * | 2002-09-05 | 2004-03-11 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
-
2005
- 2005-04-02 ES ES05007230T patent/ES2290806T3/es active Active
- 2005-04-02 EP EP05007230A patent/EP1707188B1/de active Active
- 2005-04-02 AT AT05007230T patent/ATE368446T1/de not_active IP Right Cessation
- 2005-04-02 DE DE602005001848T patent/DE602005001848T2/de not_active Expired - Fee Related
-
2006
- 2006-03-21 WO PCT/US2006/010283 patent/WO2006107594A1/en active Application Filing
- 2006-03-21 AU AU2006232897A patent/AU2006232897A1/en not_active Abandoned
- 2006-03-21 CA CA002601084A patent/CA2601084A1/en not_active Abandoned
- 2006-03-21 JP JP2008502156A patent/JP2008533176A/ja active Pending
- 2006-03-21 CN CNA2006800099241A patent/CN101151014A/zh active Pending
- 2006-03-21 BR BRPI0609557-7A patent/BRPI0609557A2/pt not_active Application Discontinuation
- 2006-03-31 US US11/395,791 patent/US20060242772A1/en not_active Abandoned
Patent Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02104778A (ja) * | 1988-09-12 | 1990-04-17 | Bristol Myers Squibb Co | 新規な染色用組成物と染色法 |
| JPH04338321A (ja) * | 1991-02-01 | 1992-11-25 | L'oreal Sa | ケラチン繊維用染色剤 |
| JPH04360818A (ja) * | 1991-03-05 | 1992-12-14 | L'oreal Sa | ケラチン繊維の染色方法および染色剤 |
| JPH04368318A (ja) * | 1991-03-05 | 1992-12-21 | L'oreal Sa | ケラチン繊維の染色方法および染色剤 |
| JPH0597778A (ja) * | 1991-10-03 | 1993-04-20 | Kawasaki Steel Corp | ２−アミノインダンおよびその塩類の製造方法 |
| JPH07508035A (ja) * | 1992-05-20 | 1995-09-07 | メルク エンド カンパニー インコーポレーテッド | ４−アザステロイド５α−レダクターゼ阻害剤 |
| JPH08509479A (ja) * | 1993-04-30 | 1996-10-08 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチェン | ケラチン含有繊維を染色するためのイサチン誘導体 |
| JPH09510226A (ja) * | 1994-03-17 | 1997-10-14 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのイサチン誘導体 |
| JP2001519369A (ja) * | 1997-10-14 | 2001-10-23 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのインダノン化合物の使用 |
| JP2003518481A (ja) * | 1999-12-24 | 2003-06-10 | ヘンケル・コマンディットゲゼルシャフト・アウフ・アクチエン | ケラチン含有繊維を染色するためのメチルキノリニウム化合物の使用 |
| JP2003532743A (ja) * | 2000-05-10 | 2003-11-05 | ウエラ アクチェンゲゼルシャフト | 繊維を染色する薬剤及び繊維を一時的に染色するための方法 |
| JP2003128635A (ja) * | 2001-10-16 | 2003-05-08 | Koei Chem Co Ltd | 不飽和アミン類の製造方法 |
| JP2005523914A (ja) * | 2002-04-26 | 2005-08-11 | ウエラ アクチェンゲゼルシャフト | ケラチン繊維の酸化染色剤 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1707188A1 (de) | 2006-10-04 |
| WO2006107594A8 (en) | 2007-11-08 |
| ES2290806T3 (es) | 2008-02-16 |
| CN101151014A (zh) | 2008-03-26 |
| DE602005001848T2 (de) | 2008-04-17 |
| CA2601084A1 (en) | 2006-10-12 |
| BRPI0609557A2 (pt) | 2010-04-13 |
| ATE368446T1 (de) | 2007-08-15 |
| DE602005001848D1 (de) | 2007-09-13 |
| EP1707188B1 (de) | 2007-08-01 |
| WO2006107594A1 (en) | 2006-10-12 |
| US20060242772A1 (en) | 2006-11-02 |
| AU2006232897A1 (en) | 2006-10-12 |
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